Derivatives of sulindac can protect normal cells against oxidative damage

a sulindac and normal cell technology, applied in the direction of antinoxious agents, drug compositions, cardiovascular disorders, etc., can solve the problems of ros can cause oxidative damage to cells and tissues, limited long-term use of non-steroidal anti-inflammatory drugs such as sulindac, and significant toxicity of sulindac sulfone relative to sulindac, etc., to achieve no cox inhibitory activity, increase intracellular cgmp and/or camp

Active Publication Date: 2021-11-30
UNIV OF SOUTH ALABAMA
View PDF11 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0010]An additional aspect of the present invention provides a method of preventing or reducing the extent of tissue damage of an ischemic event in a subject at elevated risk of an ischemic event, the method involving identifying a subject at elevated risk of an ischemic event and administering a therapeutically effective amount of the compound (Z)-2-(5,6-dimethoxy-2-methyl-1-(3,4,5-trimethoxybenzylidene)-1H-inden-3-yl)acetic acid, or a pharmaceutically acceptable salt or prodrug thereof to the subject, thereby preventing or reducing the extent of tissue damage of an ischemic event in the subject identified as being at elevated risk of an ischemic event.

Problems solved by technology

While low levels of ROS are present under normal physiological conditions, in excess, ROS can cause oxidative damage to cells and tissues by, for example, oxidizing cellular macromolecules such as nucleic acids, lipids and proteins.
Cumulative damage to cells in this manner can result in pathology.
Long term uses of nonsteroidal anti-inflammatory drugs (NSAIDS) such as sulindac are limited by gastrointestinal, renal and cardiovascular toxicities, which are caused by the inhibition of COX-1 and COX-2 and suppression of physiologically important prostaglandins.
However, sulindac sulfone is significantly more toxic to cells relative to sulindac.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Derivatives of sulindac can protect normal cells against oxidative damage
  • Derivatives of sulindac can protect normal cells against oxidative damage
  • Derivatives of sulindac can protect normal cells against oxidative damage

Examples

Experimental program
Comparison scheme
Effect test

working examples

[0133]The present invention is now described in terms of the following non-limiting examples.

example 1

Materials and Methods

[0134]Chemical synthesis of Compound 9: 3,4-Dimethoxybenzaldehyde was treated with propionic anhydride and sodium propionate at 130° C. for 36 h to give (Z)-3-(3,4-dimethoxyphenyl)-2-methylacrylic acid as a colorless solid. Catalytic hydrogenation at 40 psi afforded 3-(3,4-dimethoxyphenyl)-2-methylpropanoic acid as colorless oil. 5,6-Dimethoxy-2-methyl-2,3-dihydro-1H-inden-1-one was obtained by treating the oil with polyphosphoric acid (PPA) at 50° C. for 20 min, followed by a standard purification procedure; the ketone was refluxed with 2-cyanoacetic acid, acetic acid and ammonium chloride in toluene for 36h, followed by hydrolysis with potassium hydroxide in 60% of ethanol to give 2-(5,6-dimethoxy-2-methyl-1H-inden-3-yl)acetic acid. Reaction of the acid with 3,4,5-trimethoxybenzaldehyde and methoxide in methanol at 85° C. overnight afforded 2-(5,6-dimethoxy-2-methyl-1-(3,4,5-trimethoxybenzyl)-1H-inden-3-yl)acetic acid (Compound 9) as a yellow solid.

[0135]Chemi...

example 2

Identification and Initial Evaluation of Indene Derivatives

[0144]Sulindac is a known NSAID that has been shown to have anti-cancer activity in experimental rodent models of tumorigenesis and is effective for the treatment of precancerous colonic adenomas in patients with familial adenomatous polyposis (15-17). However, sulindac, like other NSAIDs, has gastrointestinal and other toxicities resulting from COX inhibition that may limit their long-term use for cancer chemoprevention or other diseases. To develop safer and more efficacious derivatives, previous studies have focused primarily on synthesizing derivatives that have reduced COX inhibitory activity and improve potency to inhibit tumor cell growth (18, 19). As shown previously, sulindac can also protect normal cells against oxidative damage by initiating a protective preconditioning response (9, 10) that is independent of its COX inhibitory activity. Since the protective effect observed with sulindac using cells in culture req...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
emission wavelengthaaaaaaaaaa
excitation wavelengthaaaaaaaaaa
weightaaaaaaaaaa
Login to view more

Abstract

The disclosure provides chemical compounds possessing therapeutic and / or protective properties against oxidative damage. Methods of making such therapeutic and / or protective compounds and associated compositions are also provided, as are methods for their use, which include protecting cells from oxidative damage and / or inhibiting production of ROS in a cell or subject, as well as preventing or reducing the extent of tissue damage caused by an ischemic event in a subject at elevated risk of such an event.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a U.S. National Phase entry under 35 U.S.C. § 371 of International Application No. PCT / US2018 / 022885, filed Mar. 16, 2017, published in English, which claims the benefit of priority under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 62 / 472,785, filed on Mar. 17, 2017, entitled, “Derivatives of Sulindac Can Protect Normal Cells Against Oxidative Damage”. The contents of these related applications are incorporated herein by reference in their entireties.GOVERNMENTAL SUPPORT[0002]Development of the present invention was supported, at least in part, by the National Cancer Institute of the National Institutes of Health under Award Number 1R01CA131378. Therefore, the Government may have certain rights in the invention.BACKGROUND OF THE INVENTION[0003]Oxygen is involved in a wide range of normal metabolic reactions and is essential for the survival of all aerobic organisms, including human beings. Reactive oxygen sp...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Patents(United States)
IPC IPC(8): C07C59/72A61P9/10
CPCC07C59/72A61P9/10A61K31/192A61P39/06A61P27/02A61K45/06A61K31/616A61K31/155C07C2602/24A61K2300/00
Inventor PIAZZA, GARYCHEN, XIWEISSBACH, HERBERTALLANI, SHAILAJA KESRAJU
Owner UNIV OF SOUTH ALABAMA
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products